Bis-esters of methanediol with penicillins and penicillanic acid 1,1-dioxide

ABSTRACT

6&#39;-Acylaminopenicillanoyloxymethyl esters of penicillanic acid 1,1-dioxide are useful as antibacterial agents. The 6&#39;-aminopenicillanoyloxymethyl ester, halomethyl esters, alkylsulfonyloxymethyl esters and arylsulfonyloxymethyl esters of penicillanic acid 1,1-dioxide are all useful intermediates for the aforesaid antibacterial agents.

This application is a division of application Ser. No. 039,539, filedMay 16, 1979 and now U.S. Pat. No. 4,244,951.

BACKGROUND OF THE INVENTION

This invention relates to new chemical compounds. More particularly itrelates to new chemical compounds which are of value as antibacterialagents. These new antibacterial agents are bis-esters of methanediol, inwhich one hydroxy group of the methanediol has been esterified with thecarboxy group of a 6-acylaminopenicillanic acid compound, and the otherhydroxy group of the methanediol has been esterified with the carboxygroup of penicillanic acid 1,1-dioxide.

In addition, this invention relates to the6'-aminopenicillanoyloxymethyl ester, halomethyl esters,alkylsulfonyloxymethyl esters and arylsulfonyloxymethyl esters ofpenicillanic acid 1,1-dioxide. The latter compounds are usefulintermediates to the antibacterial agents of this invention.

West German Offenlegungsschrift No. 2,824,535, published Dec. 14, 1978,and Iranian Pat. No. 19,601, granted July 12, 1978, disclosepenicillanic acid 1,1-dioxide, and esters thereof readily hydrolyzablein vivo, as antibacterial agents and as betalactamase inhibitors.Penicillanic acid 1,1-dioxide and esters thereof readily hydrolyzable invivo increase the antibacterial effectiveness of certain penicillin andcephalosporin compounds against certain bacteria.

Belgian Pat. No. 764,688, granted Mar. 23, 1971, discloses: (a) certain6'-acylaminopenicillanoyloxymethyl 6-acylaminopenicillanates; (b)certain 6'-acylaminopenicillanoyloxymethyl 6-aminopenicillanates; (c)6'-aminopenicillanoyloxymethyl 6-aminopenicillanate; and (d)chloromethyl 6-aminopenicillanate. U.S. Pat. No. 3,850,908 discloseschloromethyl esters of several natural, biosynthetic and semi-syntheticpenicillin compounds.

The antibacterial agents of the present invention are efficientlyabsorbed from the gastrointestinal tract of mammals, and afterabsorption they are transformed into a 6-acylaminopenicillanic acid andpenicillanic acid 1,1-dioxide.

SUMMARY OF THE INVENTION

This invention provides new antibacterial agents of the formula ##STR1##and the pharmaceutically-acceptable salts thereof, wherein R¹ is an acylgroup of an organic carboxylic acid. However, preferred compounds of theformula I are those in which R¹ is an acyl group known from a natural,biosynthetic or semisynthetic penicillin compound. Especially preferredcompounds of the formula I are those in which R¹ is selected from thegroup consisting of 2-phenylacetyl, 2-phenoxyacetyl,2-amino-2-phenylacetyl, 2-amino-2-[4-hydroxyphenyl]acetyl,2-carboxy-2-phenylacetyl, 2-carboxy-2-[2-thienyl]acetyl,2-carboxy-2-[3-thienyl]acetyl,2-[4-ethyl-2,3-dioxopiperazinocarbonylamino]-2-phenylacetyl and a groupof the formula ##STR2## wherein R³ is selected from the group consistingof hydrogen, alkanoyl having from two to four carbons and alkylsulfonylhaving from one to three carbons.

Preferred individual compounds of formula I are:

6'-(2-phenylacetamido)penicillanoyloxymethyl penicillanate 1,1-dioxide,

6'-(2-phenoxyacetamido)penicillanoyloxymethyl penicillanate 1,1-dioxide,

6'-(2-amino-2-phenylacetamido)penicillanoyloxymethyl penicillanate1,1-dioxide and

6-(2-amino-2-[4-hydroxyphenyl]acetamido)penicillanoyloxymethylpenicillanate 1,1-dioxide.

This invention also provides compounds of the formula: ##STR3## and thesalts thereof, wherein X is a good leaving group. Examples of X arechloro, bromo, iodo, alkylsulfonyloxy having from one to four carbonatoms, benzenesulfonyloxy and toluenesulfonyloxy. The compounds offormulae III and IV are useful as intermediates to the antibacterialagents of the invention.

DETAILED DESCRIPTION OF THE INVENTION

This invention relates to derivatives of penicillanic acid, which isrepresented by the following structural formula ##STR4## In formula V,broken line attachment of a substituent to the bicyclic nucleusindicates that the substituent is below the plane of the bicyclicnucleus. Such a substituent is said to be in the alpha-configuration.Conversely, solid line attachment of a substituent to the bicyclicnucleus indicates that the substituent is attached above the plane ofthe nucleus. This latter configuration is referred to as thebeta-configuration.

Using this system, the compounds of formulae I and III are named asderivatives of penicillanoyloxymethyl penicillanate (VA), in whichprimed and unprimed locants are used to distinguish between the two ringsystems, viz: ##STR5##

Additionally, throughout this specification, whenever reference is madeto a compound which has a 2-amino-2-(substituted)acetamido or2-(substituted amino)-2-(substituted)acetamido group at the 6-positionof a penicillanic acid derivative, it is to be understood that thisrefers to a compound in which said 2-amino-2-(substituted)acetamido or2-(substituted amino)-2-(substituted)acetamido has the D-configuration.

In one method according to the invention a compound of formula I can beprepared by reacting a carboxylate salt of the formula ##STR6## with acompound of the formula ##STR7## wherein R¹ and X as previously defined,and M is a carboxylate salt forming cation. A variety of cations can beused to form the carboxylate salt in the compound of formula VI, butsalts which are commonly used include: alkali metal salts, such assodium and potassium salts; alkaline earth metal salts, such as calciumand barium salts; and tertiary amine salts, such as trimethylamine,triethylamine, tributylamine, diisopropylethylamine, N-methylmorpholine,N-methylpiperidine, N-methylpyrrolidine, N,N'-dimethylpiperazine and1,2,3,4-tetrahydroquinoline.

The reaction between a compound of formula VI and a compound of formulaVII is usually carried out by contacting the reagents in a polar,organic solvent, at a temperature in the range from about 0° to about80° C., and preferably from 25° to 50° C. The compounds of formula VIand VII are usually contacted in substantially equimolar proportions,but an excess of either reagent, for example up to a ten-fold excess,can be used. A wide variety of solvents can be used, but it is usuallyadvantageous to use a relatively polar solvent, since this has theeffect of speeding up the reaction. Typical solvents which can be usedinclude N,N-dimethylformamide, N,N-dimethylacetamide,N-methylpyrrolidone, dimethylsulfoxide and hexamethylphosphoramide. Thereaction time varies according to a number of factors, but at about 25°C. reaction times of several hours, e.g. 12 to 24 hours, are commonlyused. When X is chloro or bromo, it is sometimes advantageous to add upto about one molar equivalent of an alkali metal iodide, which has theeffect of speeding up the reaction.

The compound of formula I is isolated in conventional fashion. When awater-miscible solvent is used, it is usually sufficient simply todilute the reaction medium with an excess of water. The product is thenextracted into a water immiscible solvent, such as ethyl acetate, andthen the product is recovered by solvent evaporation. When a waterimmiscible solvent is used, it is usually sufficient to wash the solventwith water, and then recover the product by solvent evaporation. Thecompound of formula I can be purified by well-known methods, such asrecrystallization or chromatography, but due regard must be given to thelability of the beta-lactam ring system.

When the group R¹ in a compound of formula VI contains a basic group,such as a primary amino group, this group can interfere during thereaction with the ester VII. In this case it is usually advantageous toprotect the amino group in R¹ before contacting the compound of formulaVI with the compound of formula VII. A variety of conventional aminoprotecting groups can be used for this purpose. The only requirementsfor such a group are that: (a) it can be affixed to the compound offormula VI under conditions which do not adversely affect the compoundof formula VI; (b) it is stable under the conditions under which thecompound of formula VI reacts with the compound of formula VII; and (c)it can be removed after the reaction with the compound of formula VII iscomplete, using conditions which do not adversely affect the compound offormula I. Typical amino protecting groups which can be used arebenzyloxycarbonyl, substituted benzyloxycarbonyl, 2-nitrophenylsulfenyland 2,2,2-trichloroethoxycarbonyl. Benzyloxycarbonyl and4-nitrobenzyloxycarbonyl are particularly convenient groups.

When the group R¹ in a compound of formula VI contains a carboxy group,it is usual to protect this carboxy group before the reaction with thecompound of formula VII, particularly when the carboxy group is subjectto ready decarboxylation. In this case it is advantageous to start witha compound of formula VI in which the carboxy group in R¹ is in the formof a readily hydrolyzable ester, e.g. a phenyl or substituted phenylester. After the coupling with the compound of formula VII is complete,the free carboxy group in R¹ is liberated by mild, alkaline hydrolysis,e.g. using the technique disclosed in U.S. Pat. No. 3,679,801. Thismethodology is especially useful when R¹ is a group such as2-carboxy-2-phenylacetyl, 2-carboxy-2-[thienyl]acetyl, etc.

A variation of the foregoing method of preparing a compound of formula Iinvolves reaction of a compound of the formula ##STR8## with a compoundof the formula ##STR9## wherein M and X are as defined previously, andR² is the group R¹, but with any free amino groups and/or carboxy groupsprotected, followed if necessary by removal of any amino or carboxyprotecting group. In the compounds of formula IX, the free amino groupsand the carboxy groups are protected with exactly the same protectinggroups as described earlier for the compound of formula VI. The reactionbetween a compound of formula VIII and IX is carried out in exactly thesame manner that is used for the reaction of a compound of formula VIwith a compound of formula VII. Finally, any amino and/or carboxyprotecting groups are removed, and these are removed in conventionalmanner for the group involved.

In another method according to the invention, a compound of formula Ican be prepared by acylation of the compound of formula III with anactivated derivative of an acid of the formula R² --COOH, wherein R² isas previously defined, followed if necessary by removal of any aminoand/or carboxy protecting groups from R². This converts the moiety R²--CO into the moiety R¹ --CO.

The acylation reaction is usually conducted in a reaction-inert solventsystem. In a typical acylation procedure, from about 0.5 to about threemolar equivalents of the activated derivative of the acid of formula R²--COOH is contacted with the compound of formula III, in areaction-inert solvet system, at a temperature in the range from about-40° to about 30° C., and preferably from about -10° to about 10° C. Thepreferred ratio of activated derivative to compound of formula III is1.0:1.0 to 1.2:1.0. Reaction-inert solvents which are commonly used inthis acylation are: chlorinated hydrocarbons, such as chloroform anddichloromethane; ethers, such as diethyl ether and tetrahydrofuran; lowmolecular weight esters, such as ethyl acetate and butyl acetate; lowmolecular weight aliphatic ketones, such as acetone and methyl ethylketone; tertiary amides, such as N,N-dimethylformamide andN-methylpyrrolidone; acetonitrile; water; and mixtures thereof. Whenaqueous or partially aqueous solvent systems are used, the pH should bemaintained in the range from about 4 to about 9, and preferably about 7.

An activated derivative of the acid of the formula R² --COOH which iscommonly used is an acid halide, e.g. the acid chloride. In thisinstance it is preferable, though not essential, to carry out theacylation in the presence of an acid binder. Suitable acid binders aretertiary amines such as trialkylamines, e.g. triethylamine,N-methylmorpholine, N,N-dimethylaniline, pyridine and the like, orbicarbonates such as potassium bicarbonate or sodium bicarbonate. Buffersystems such as phosphate buffers can also be used.

Other activated derivatives of the acid of formula R² --COOH which canbe used are active esters. Examples of active esters are phenyl esters,such as 4-nitrophenyl and 2,4,5-trichlorophenyl esters; thio esters,such as thiol methyl and thiol phenyl esters; and N-hydroxy esters, suchas N-hydroxysuccinimide and N-hydroxyphthalimide esters. These activeesters are prepared by methods well-known in the art. In many cases, theactive ester can be replaced by the corresponding acid azide, or by theimidazole or triazole amide.

Another method for activation of the acid of formula R² --COOH involvesmixed anhydride formation, i.e. mixed carboxylic-carbonic and mixeddicarboxylic anhydride formation. In the case of mixed carboxyliccarbonic anhydrides, a carboxylate salt of the acid of formula R² --COOHis usually reacted with a lower-alkyl chloroformate, e.g. ethylchloroformate; in the case of a mixed dicarboxylic anhydride, acarboxylate salt of the acid of formula R² --COOH is usually reactedwith a hindered lower-alkanoyl chloride. e.g. pivaloyl chloride.

In addition to the above, the acid of formula R² --COOH can be activatedby contacting the acid with a peptide coupling agent, according tostandard procedures. Such agents include carbodiimides, for exampledicyclohexylcarbodiimide, alkoxyacetylenes, for example methoxyacetyleneand ethoxyacetylene, and N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline.

The protecting groups used to protect amino or carboxy groups in acompound of formula R² --COOH are those conventionally used duringacylation of a 6-aminopenicillanic acid derivative. Protecting groupswhich are particularly useful for amino groups are the benzyloxycarbonylgroup, the 4-nitrobenzyloxycarbonyl group and the enamines formed bycondensation with a beta-dicarbonyl compound such as an alkylacetoacetate. After the acylation step, the amino protecting group isremoved in conventional fashion. When the acid of formula R² --COOH isto be activated as an acid halide e.g. acid chloride, an especiallyconvenient manner of protecting an amino group involves salt formation,e.g. formation of a hydrochloride salt.

The compounds of formula VI are known antibiotics, which are prepared bythe published procedures.

The compounds of formula VII are prepared from the compounds of formulaVIII by reaction with a compound of formula Y--CH₂ --X, wherein X and Yare each good leaving groups, e.g. chloro, bromo, iodo,alkylsulfonyloxy, benenesulfonyloxy or toluenesulfonyloxy. The sameconditions that were described previously for reaction of a compound offormula VII with a compound of formula VI are used for this invention,except that it is preferable to use an excess of the compound of formulaX--CH₂ --Y (e.g. a four-fold excess).

In like manner, the compounds of formula IX are prepared by reaction ofa compound of formula ##STR10## with a compound of formula Y--CH₂ --X,wherein R², M, Y and X are as previously defined. The conditions usedare the same as those described previously for reaction of a compound offormula VIII with a compound of formula X--CH₂ --Y.

The compound of formula III can be prepared by a three-step procedurewhich comprises: (a) conversion of 6-aminopenicillanic acid into a6-(protected amino)penicillanic acid; (b) reaction of a salt of the6-(protected amino)penicillanic acid with a compound of formula VII; and(c) removal of the amino protecting group. A wide variety of aminoprotecting groups can be used for this purpose, and typical examples arebenzyloxycarbonyl, 4-nitrobenzyloxycarbonyl and2,2,2-trichloroethoxycarbonyl. Steps (a) and (c) are carried out inconventional fashion, and step (b) is carried out in exactly the samemanner that was described previously for reaction of a compound offormula VII with a compound of formula VI.

Alternatively, the compound of formula III can be prepared by afour-step procedure which comprises (i) conversion of6-aminopenicillanic acid into a 6-(protected amino)penicillanic acid;(ii) reaction of a salt of the 6-(protected amino)penicillanic acid witha compound of formula X--CH₂ --Y, wherein X and Y are as previouslydefined; (iii) reaction of the product of step (ii) with a compound offormula VIII; and (iv) removal of the amino protecting group. A widevariety of amino protecting groups can be used for this purpose, andtypical examples are benzyloxycarbonyl, 4-nitrobenzyloxycarbonyl and2,2,2-trichloroethoxycarbonyl. Steps (i) and (iv) are carried out inconventional fashion; step (ii) is carried out in exactly the samemanner that was described previously for reaction of a compound offormula VIII with a compound of formula X--CH₂ --Y; and step (iii) iscarried out in exactly the same manner that was described previously forreaction of a compound of formula VI with a compound of formula VII.

Penicillanic acid 1,1-dioxide and the salts thereof are prepared bypublished procedures (see West German Offenlegungsschrift 2,824,535).

Those compounds of formula I which have a basic function, e.g. an aminogroup, in the group R¹ will form acid addition salts, and these acidaddition salts are considered to be within the scope and purview of thisinvention. Said acid addition salts are prepared by standard methods forpenicillin compounds, for example by combining a solution of thecompound of formula I in a suitable solvent (e.g. water, acetone,methanol, ethanol or butanol) with a solution containing astoichiometric equivalent of the appropriate acid. If the saltprecipitates, it is recovered by filtration. Alternatively, it can berecovered by evaporation of the solvent, or, in the case of aqueoussolutions, by lyophilization. Of particular value are the sulfate,hydrochloride, hydrobromide, nitrate, phosphate, citrate, tartrate,pamoate, perchlorate, sulfosalicylate and 4-toluenesulfonate salts.

Those compounds of formula I which have an acidic function, e.g. acarboxyl group, in the group R¹ will form base salts, and these basesalts are to be considered within the scope and purview of thisinvention. The base salts are prepared by standard methods forpenicillin compounds, for example by contacting the acidic and basiccomponents in a stoichiometric ratio, in an aqueous, non-aqueous orpartially aqueous medium, as appropriate. They are then recovered byfiltration, by precipitation with a non-solvent followed by filtration,by evaporation of the solvent, or, in the case of aqueous solutions, bylyophilization, as appropriate. Basic agents which are suitably employedin salt formation belong to both the organic and inorganic types, andthey include ammonia, organic amines, alkali metal hydroxides,carbonates, bicarbonates, hydrides and alkoxides, as well as alkalineearth metal hydroxides, carbonates, hydrides and alkoxides.Representative examples of such bases are primary amines, such asn-propylamine, n-butylamine, aniline, cyclohexylamine, benzylamine,p-toluidine and octylamine; secondary amines, such as diethylamine,N-methylaniline, morpholine, pyrrolidine and piperidine; tertiaryamines, such as triethylamine, N,N-dimethylaniline, N-ethylpiperidine,N-methylmorpholine and 1,5-diazabicyclo[4.3.0]non-5-ene; hydroxides,such as sodium hydroxide, potassium hydroxide, ammonium hydroxide andbarium hydroxide; alkoxides, such as sodium ethoxide and potassiumethoxide; hydrides, such as calcium hydride and sodium hydride;carbonates, such as potassium carbonate and sodium carbonate; andbicarbonates, such as sodium bicarbonate and potassium bicarbonate.

When contemplating therapeutic use for a salt of an antibacterialcompound of this invention, it is necessary to use apharmaceutically-acceptable salt; however, salts other than these can beused for a variety of purposes. Such purposes include isolating andpurifying particular compounds, and interconvertingpharmaceutically-acceptable salts and their non-salt counterparts.

The compounds of formula I possess in vivo antibacterial activity inmammals, and this activity can be demonstrated by standard techniquesfor penicillin compounds. For example, the compound of formula I isadministered to mice in which acute infections have been established byintraperitoneal inoculation with a standardized culture of a pathogenicbacterium. Infection severity is standardized such that the mice receiveone to ten times the LD₁₀₀ (LD₁₀₀ : the minimum inoculation required toconsistently kill 100 percent of control mice). At the end of the test,the activity of the compound is assessed by counting the number ofsurvivors which have been challenged by the bacterium and also havereceived the compound of formula I. The compounds of formula I can beadministered by both the oral (p.o.) and subcutaneous (s.c.) route.

The in vivo activity of the antibacterial compounds of this inventionmakes them suitable for the control of bacterial infections in mammals,including man, by both the oral and parenteral modes of administration.The compounds are useful in the control of infections caused bysusceptible bacteria in human subjects. In general, it is thesubstitutent R¹ which determines whether a given bacterium will besusceptible to a given compound of formula I. A compound of formula Ibreaks down to the corresponding compound of formula VI (or free acidthereof) and penicillanic acid 1,1-dioxide after administration to amammalian subject by both the oral and parenteral route. Penicillanicacid 1,1-dioxide then functions as a beta-lactamase inhibitor, and itincreases the antibacterial effectiveness of the compound of formula VI(or free acid thereof). For example, when R¹ is 2-phenylacetyl or2-phenoxyacetyl, the compounds will find use in the control ofinfections caused by susceptible strains of Staphylococcus aureus; whenR¹ is D-2-amino-2-phenylacetyl, D-2-amino-2-[4-hydroxyphenyl]acetyl,2-carboxy-2-phenylacetyl, 2-carboxy-2 -[2-thienyl]acetyl,2-carboxy-2-[3-thienyl]acetyl,2-[4-ethyl-2,3-dioxopiperazinocarbonylamino]-2-phenylacetyl or a groupof formula II, the compounds are useful in the control of infectionscaused by susceptible strains of Escherichia coli.

In determining whether a particular strain of Staphylococcus aureus orEscherichia coli is sensitive to a particular compound of formula I, thein vivo test described earlier can be used. Alternatively, the minimuminhibitory concentration (MIC) of a 1:1 mixture of the compound offormula VI (or its corresponding free acid) and the compound of formulaVIII (or its corresponding free acid) can be measured. The MIC's can bemeasured by the procedure recommended by the International CollaborativeStudy on Antibiotic Sensitivity Testing (Ericcson and Sherris, ActaPathologica et Microbiologia Scandinav, Supp. 217, Section B: 64-68[1971]), which employs brain heart infusion (BHI) agar and the inoculareplicating device. Overnight growth tubes are diluted 100 fold for useas the standard inoculum (20,000-10,000 cells in approximately 0.002 ml.are placed on the agar surface; 20 ml. of BHI agar/dish). Twelve 2 folddilutions of the test compound are employed, with initial concentrationof the test drug being 200 mcg./ml. Single colonies are disregarded whenreading plates after 18 hrs. at 37° C. The susceptibility (MIC) of thetest organism is accepted as the lowest concentration of compoundcapable of producing complete inhibition of growth as judged by thenaked eye.

When using an antibacterial compound of this invention, or a saltthereof, in a mammal, particularly man, the compound can be administeredalone, or it can be mixed with other antibiotic substances and/orpharmaceutically-acceptable carriers or diluents. Said carrier ordiluent is chosen on the basis of the intended mode of administration.For example, when considering the oral mode of administration, anantibacterial compound of this invention can be used in the form oftablets, capsules, lozenges, troches, powders, syrups, elixirs, aqueoussolutions and suspensions, and the like, in accordance with standardpharmaceutical practice. The proportional ratio of active ingredient tocarrier will naturally depend on the chemical nature, solubility andstability of the active ingredient, as well as the dosage contemplated.In the case of tablets for oral use, carriers which are commonly usedinclude lactose, sodium citrate and salts of phosphoric acid. Variousdisintegrants such as starch, and lubricating agents, such as magnesiumstearate, sodium lauryl sulfate and talc, are commonly used in tablets.For oral administration in capsule form, useful diluents are lactose andhigh molecular weight polyethylene glycols, e.g. polyethylene glycolshaving molecular weights of from 2000 to 4000. When aqueous suspensionsare required for oral use, the active ingredient is combined withemulsifying and suspending agents. If desired, certain sweetening and/orflavoring agents can be added. For parenteral administration, whichincludes intramuscular, intraperitoneal, subcutaneous, and intravenoususe, sterile solutions of the active ingredient are usually prepared,and the pH of the solutions are suitably adjusted and buffered. Forintravenous use, the total concentration of solutes should be controlledto render the preparation isotonic.

As indicated earlier, the antibacterial compounds of this invention areof use in human subjects and the daily dosages to be used will notdiffer significantly from other, clinically-used, penicillinantibiotics. The prescribing physician will ultimately determine theappropriate dose for a given human subject, and this can be expected tovary according to the age, weight, and response of the individualpatient as well as the nature and the severity of the patient'ssymptoms. The compounds of this invention will normally be used orallyat dosages in the range from about 20 to about 100 mg. per kilogram ofbody weight per day, and parenterally at dosages from about 10 to about100 mg. per kilogram of body weight per day, usually in divided doses.In some instances it may be necessary to use doses outside these ranges.

The following examples and preparations are provided solely for furtherillustration. Infrared (IR) spectra were measured as potassium bromidediscs (KBr discs) and diagnostic absorption bands are reported in wavenumbers (cm⁻¹). Nuclear magnetic resonance spectra (NMR) were measuredat 60 MHz for solutions in deuterated chloroform (CDCl₃) or deuterateddimethyl sulfoxide (DMSO-d₆), and peak positions are reported in partsper million downfield from tetramethylsilane. The followingabbreviations for peak shapes are used: s, singlet; d, doublet; t,triplet; q, quartet, m, multiplet.

EXAMPLE 1 6'-(2-Phenylacetamido)penicillanoyloxymethyl Penicillanate1,1-Dioxide

To a stirred solution of 1.3 g. of potassium6-(2-phenylacetamido)penicillanate in 20 ml. of dimethyl sulfoxide wasadded 845 mg. of chloromethyl penicillanate 1,1-dioxide followed by afew milligrams of sodium iodide. Stirring was continued overnight at ca.25° C., and then the reaction mixture was poured into 140 ml. ofice-water. The pH was raised to 8.5, and then the mixture was extractedwith ethyl acetate. The combined ethyl acetate extracts were washed withwater, dried (Na₂ SO₄) and evaporated in vacuo. This afforded 600 mg. ofcrude material.

The crude material was chromatographed on silica gel, eluting with a 1:1mixture of ethyl acetate and hexane, and this afforded 200 mg. of thetitle compound 12% yield). The IR spectrum (KBr disc) showed anabsorption at 1783 cm⁻¹. The NMR spectrum (CDCl₃) showed absorptions at7.4 (s), 6.3 (d), 5.9 (s), 5.8-5.3 (m), 4.65 (t), 4.45 (s), 3.65 (s),3.45 (d), 1.62 (s) and 1.48-1.4 (m) ppm.

EXAMPLE 2 6'-(2-Phenoxyacetamido)penicillanoyloxymethyl Penicillanate1,1-Dioxide

A mixture of 1.4 g. of potassium 6-(2-phenoxyacetamido)penicillanate,845 mg. of chloromethyl penicillanate 1,1-dioxide, 20 ml. of dimethylsulfoxide and a few milligrams of sodium iodide was stirred at ca. 25°C. overnight. The mixture was poured into 140 ml. of ice-water and thepH was adjusted to 8.5. The resultant aqueous system was extracted withethyl acetate, and the extracts were combined, washed with water, dried(Na₂ SO₄) and evaporated in vacuo. This afforded 660 mg. of crudematerial.

The crude material was chromatographed on silica gel, using a 1:1mixture of ethyl acetate and hexane as eluant, and this afforded 230 mg.of the title product (13% yield). The IR spectrum (KBr disc) showed anabsorption at 1786 cm⁻¹. The NMR spectrum (CDCl₃) showed absorptions at7.4 (s), 5.85 (s), 5.45 (s), 5.05 (s), 4.6 (t), 4.43 (s), 4.4 (s), 3.45(d), 1.62 (s), 1.48 (s), 1.44 (s) and 1.4 (s) ppm.

EXAMPLE 3 6'-(2-Amino-2-phenylacetamido)penicillanoyloxymethylPenicillanate 1,1-Dioxide

To a solution of 1.6 g. of6'-(2-benzyloxycarbonylamino-2-phenylacetamido)penicillanoyloxymethylpenicillanate, 1,1-dioxide in 100 ml. of tetrahydrofuran and 80 ml. ofwater was added 0.12 ml. of glacial acetic acid followed by 1.6 g. of10% palladium-on-carbon. The mixture was shaken under an atmosphere ofhydrogen at a pressure of ca. 50 psig for 1.5 hours. At this point thecatalyst was removed by filtration and 1.6 g. of fresh catalyst wasadded. The mixture was shaken under hydrogen at ca. 50 psig for afurther 1 hour. The catalyst was removed by filtration and the bulk ofthe tetrahydrofuran was removed by evaporation in vacuo. The pH of theresidual aqueous phase was lowered to 2.0 using 6 N hydrochloric acidand the acidified solution was extracted with ethyl acetate. Theextracts were dried (Na₂ SO₄) and evaporated in vacuo to give 500 mg. ofimpure starting material. The pH of the above acidified solution wasraised to 8.5 and then it was further extracted with ethyl acetate. Thelatter extracts were combined, dried (Na₂ SO₄) and evaporated in vacuoto give 500 mg. of the title compound (38% yield).

EXAMPLE 46'-(2-Benzyloxycarbonylamino-2-phenylacetamido)penicillanoyloxymethylPenicillanate 1,1-Dioxide

To a stirred solution of 1.9 g. of potassium6-(2-benzyloxycarbonylamino-2-phenylacetamido)penicillanate in 30 ml. ofdimethyl sulfoxide was added 230 mg. of chloromethyl penicillanate1,1-dioxide followed by a few milligrams of sodium iodide. Stirring wascontinued at ambient temperature overnight, and then the reactionmixture was poured into 60 ml. of water. The pH was raised to 8.5 andthe product was extracted into ethyl acetate. The extracts were washedwith water and with saturated sodium chloride solution, and then theywere dried (Na₂ SO₄). Evaporation of the ethyl acetate in vacuo gave 800mg. of crude product.

The crude product was purified by chromatography on silica gel, using1:1 ethyl acetate-hexane as eluant, to give 440 mg. of the titlecompound (18% yield). The NMR spectrum of the product (CDCl₃) showedabsorptions at 7.4 (m, 10H), 7.1 (d, 1H, J=8 Hz), 6.2 (d, 1H, J=8 Hz),5.9 (s, 2H), 5.7-5.2 (m, 3H), 5.1 (s, 2H), 4.6 (t, 1H), 4.4 (s, 2H), 3.4(d, 2H) and 1.7-1.2 (m, 12H) ppm.

EXAMPLE 5 6'-(2-Amino-2-phenylacetamido)penicillanoyloxymethylPenicillanate 1,1-Dioxide

6'-(2-[4-Nitrobenzyloxycarbonylamino]-2-phenylacetamido)penicillanoyloxymethylpenicillanate 1,1-dioxide was hydrogenated in the presence of 10%palladium-on-carbon, according to the procedure of Example 3. After thehydrogenation, the catalyst was removed by filtration and the pH wasraised to 8.5. The resulting mixture was extracted with ethyl acetate,and then the extracts were combined, dried using sodium sulfate andevaporated in vacuo. The residue was dissolved in 3 ml. of ethylacetate, and the resulting solution was added dropwise to 40 ml. ofhexane. The solid which precipitated was recovered by filtration to give500 mg. of crude product.

The crude product was purified by chromatography on silica gel, usingethyl acetate as eluant, to give a 40% yield of the title compound. TheIR spectrum (KBr disc) showed an absorption at 1802 cm⁻¹. The NMRspectrum (CDCl₃) showed absorptions at 8.1 (d, 1H, J=6 Hz), 7.4 (s, 4H),5.9 (q, 2H), 5.7-5.5 (m, 2H), 4.75-4.6 (m, 2H), 4.55 (s, 1H), 4.45 (s,1H), 3.55 (d, 2H), 1.6 (d, 6H) and 1.5 (d, 6H) ppm.

EXAMPLE 66'-(2-[4-Nitrobenzyloxycarbonylamino]-2-phenylacetamido)penicillanoyloxymethylPenicillanate 1,1-Dioxide

The title compound was prepared from potassium6-(2-[4-nitrobenzyloxycarbonylamino]-2-phenylacetamido)penicillanate andchloromethyl penicillanate 1,1-dioxide using the procedure of Example 4,except that the reaction mixture was heated at 45° C. for 3 hours afterbeing allowed to stir overnight at ambient temperature. Afterchromatography on silica gel, a 24% yield of product was obtained. TheNMR spectrum (CDCl₃) showed absorptions at 8.2 (d, 2H, J=8 Hz), 7.7-7.4(m, 7H), 6.9 (d, 2H, J=8 Hz), 5.9 (s, 2H), 5.8-5.3 (m, 3H), 5.2 (s, 2H),4.7 (t, 1H), 4.5 (s, 2H), 3.5 (d, 2H) and 1.7-1.4 (m, 12H) ppm.

EXAMPLE 76'-(2-Amino-2-[4-Hydroxyphenyl]acetamido)penicillanoyloxymethylPenicillanate 1,1-Dioxide

To a solution of 700 mg. of6'-(2-[4-nitrobenzyloxycarbonylamino]-2-[4-hydroxyphenyl]acetamido)penicillanoyloxymethylpenicillanate 1,1-dioxide in 25 ml. of water and 35 ml. oftetrahydrofuran was added 700 mg. of 10% palladium-on-carbon. Thismixture was shaken under an atmosphere of hydrogen at ca. 50 psig for 70minutes. The catalyst was removed by filtration and then the bulk of thetetrahydrofuran was removed by evaporation in vacuo. The remainingaqueous phase was basified to pH 8.5, and then it was extracted withethyl acetate. The extracts were washed with water and with saturatedsodium chloride solution, and then they were dried (Na₂ SO₄) andevaporated in vacuo. The residue was dissolved in 3 ml. of ethylacetate, and this solution was added dropwise to an excess of hexane.The solid which precipitated was recovered by filtration and dried togive 300 mg. of the title compound (56% yield).

The above product was combined with additional material of similarpurity and chromatographed on silica gel using ethyl acetate as theeluant. The appropriate column fractions were combined and evaporated invacuo, and the residue was dissolved in a small volume of ethyl acetate.The latter solution was then added dropwise to an excess of hexane, andthe solid which precipitated was recovered by filtration. The IRspectrum (KBr disc) of the material so obtained showed an absorption at1786 cm⁻¹. The NMR spectrum (CDCl₃ /DMSO-d₆) showed absorptions at7.4-6.6 (m, 4H), 5.9 (s, 1H), 5.8-5.4 (m, 2H), 4.8-4.3 (m, 4H), 3.5 (d,2H) and 1.5 (m, 12H) ppm.

EXAMPLE 86'-(2-[4-Nitrobenzyloxycarbonylamino]-2-[4-hydroxyphenyl]acetamido)penicillanoyloxymethylPenicillanate 1,1-Dioxide

A solution of 7.0 g. of potassium6-(2-[4-nitrobenzyloxycarbonylamino]-2-[4-hydroxyphenyl]acetamido)penicillanateand 3.0 g. of chloromethyl penicillanate 1,1-dioxide in 40 ml. ofdimethyl sulfoxide was heated at 45° C. for 4.5 hours. The solution wasthen poured into 120 ml of water and the pH was adjusted to 8.5. Theresulting mixture was extracted with ethyl acetate, and the combinedextracts were washed with water and with saturated sodium chloridesolution and then they were dried (Na₂ SO₄). The dried solution wasevaporated in vacuo to give 2.0 g. of crude product.

The crude product was purified by chromatography on silica gel using1.5:1 ethyl acetate-hexane as eluant. This afforded 720 mg. (9% yield)of material which showed only a single spot when assayed by thin-layerchromatography.

EXAMPLE 9

The procedure of Example 1 is repeated, except that the potassium6-(2-phenylacetamido)penicillanate is replaced by:

potassium6-(2-[4-ethyl-2,3-dioxopiperazinocarbonylamino]-2-phenylacetamido)penicillanate,

potassium6-(2-[2-oxoimidazolidinocarbonylamino]-2-phenylacetamido)penicillanate,

potassium6-(2-[3-acetyl-2-oxoimidazolidinocarbonylamino]-2-phenylacetamido)penicillanate,

potassium6-(2-[3-butyryl-2-oxoimidazolidinocarbonylamino]-2-phenylacetamido)penicillanate,

potassium6-(2-[3-methylsulfonyl-2-oximidazolidinocarbonylamino]-2-phenylacetamido)penicillanateand

potassium6-(2-[3-isopropylsulfonyl-2-oxoimidazolidinocarbonylamino]-2-phenylacetamido)penicillanate,respectively. This affords:

6'-(2-[4-ethyl-2,3-dioxopiperazinocarbonylamino]-2-phenylacetamido)penicillanoyloxymethylpenicillanate 1,1-dioxide,

6'-(2-[2-oxoimidazolidinocarbonylamino]-2-phenylacetamido)penicillanoyloxymethylpenicillanate 1,1-dioxide,

6'-(2-[3-acetyl-2-oxoimidazolidinocarbonylamino]-2-phenylacetamido)penicillanoyloxymethylpenicillanate 1,1-dioxide,

6'-(2-[3-butyryl-2-oxoimidazolidinocarbonylamino]-2-phenylacetamido)penicillanoyloxymethylpenicillanate 1,1-dioxide,

6'-(2-[3-methylsulfonyl-2-oxoimidazolidinocarbonylamino]-2-phenylacetamido)penicillanoyloxymethylpenicillanate 1,1-dioxide and

6'-(2-[3-isopropylsulfonyl-2-oxoimidazolidinocarbonylamino]-2-phenylacetamido)penicillanoyloxymethylpenicillanate, 1,1-dioxide, respectively.

EXAMPLE 10

The procedure of Example 2 is repeated, except that the chloromethylpenicillanate 1,1-dioxide used therein is replaced by an equimolaramount of:

bromomethyl penicillanate 1,1-dioxide,

iodomethyl penicillanate 1,1-dioxide,

methylsulfonyloxymethyl penicillanate, 1,1-dioxide,

isobutylsulfonyloxymethyl penicillanate 1,1-dioxide,

benzenesulfonyloxymethyl penicillanate 1,1-dioxide and

4-toluenesulfonyloxymethyl penicillanate 1,1-dioxide, respectively. Ineach case, this affords 6'-(2-phenoxyacetamido)penicillanoyloxymethylpenicillanate 1,1-dioxide.

EXAMPLE 116'-(2-Benzyloxycarbonylamino-2-phenylacetamido)penicillanoyloxymethylPenicillanate 1,1-Dioxide

A mixture of 570 mg. of chloromethyl6-(2-benzyloxycarbonylamino-2-phenylacetamido)penicillanate, 324 mg. ofsodium penicillanate 1,1-dioxide, a few milligrams of sodium iodide and20 ml. of dimethyl sulfoxide was stirred at room temperature overnight.The reaction mixture was added to 80 ml. of water, and the pH was raisedto 8.5. The product was extracted into ethyl acetate. The extract waswashed with water and with saturated sodium chloride solution, and thenit was dried (Na₂ SO₄). Evaporation in vacuo then afforded 360 mg. ofthe title compound.

EXAMPLE 126'-(2-[4-Nitrobenzyloxycarbonylamino]-2-phenylacetamido)penicillanoyloxymethylPenicillanate 1,1-Dioxide

A mixture of 500 mg. of chloromethyl6-(2-[4-nitrobenzyloxycarbonylamino]-2-phenylacetamido)penicillanate,245 mg. of sodium penicillanate 1,1-dioxide, a few milligrams of sodiumiodide and 10 ml. of dimethyl sulfoxide was stirred at room temperatureovernight. At this point, an additional 83 mg. of sodium penicillanate1,1-dioxide was added. Stirring was continued for 4 hours, and then thereaction mixture was poured into water. The aqueous system was basifiedto pH 8.5, and then it was extracted with ethyl acetate. The extractswere combined, washed with water and with saturated sodium chloridesolution, and then they were dried (Na₂ SO₄). Evaporation in vacuo thenafforded 430 mg. of the title compound, contaminated with somechloromethyl6-(2-[4-nitrobenzyloxycarbonylamino]-2-phenylacetamido)penicillanate.

EXAMPLE 136'-(2-[4-Nitrobenzyloxycarbonylamino]-2-[4-hydroxyphenyl]acetamido]penicillanoyloxymethylPenicillanate 1,1-Dioxide

A solution of 2.07 g. of chloromethyl6-(2-[4-nitrobenzyloxycarbonylamino]-2-[4-hydroxyphenyl]acetamido)penicillanate,1.1 g. of sodium penicillanate 1,1-dioxide, and a few milligrams ofsodium iodide in 30 ml. of dimethyl sulfoxide was maintained at 45° C.for 5 hours. The reaction mixture was added to 100 ml. of water and pHwas raised to 8.5. The product was extracted into ethyl acetate. Theextracts were combined, washed with water and with saturated sodiumchloride solution, and then they were dried (Na₂ SO₄). Evaporation invacuo then afforded 1.6 g. of crude product.

The crude product was chromatographed on silica gel using 1.5:1 ethylacetate-hexane as eluant, to give 550 mg. (18% yield) of the titlecompound. The NMR spectrum (CDCl₃ /DMSO-d₆) showed absorptions at 8.4(d, 1H, J=8 Hz), 8.1 (d, 2H, J=8 Hz), 7.7-6.6 (m, 7H), 5.9 (s, 2H),5.7-5.2 (m, 3H), 5.2 (s, 2H), 4.7 (t, 1H), 4.4 (d, 2H) and 1.5 (d, 12H)ppm.

EXAMPLE 14

Chloromethyl 6-(2-phenylacetamido)penicillanate and chloromethyl6-(2-phenoxyacetamido)penicillanate are reacted with sodiumpenicillanate 1,1-dioxide, according to the procedure of Example 11.This affords:

6'-(2-phenylacetamido)penicillanoyloxymethyl penicillanate 1,1-dioxideand

6'-(2-phenoxyacetamido)penicillanoyloxymethyl penicillanate 1,1-dioxide,

respectively.

EXAMPLE 15 6'-(2-Phenylacetamido)penicillanoyloxymethyl Penicillanate1,1-Dioxide

To a stirred solution of 4.62 g. of 6'-aminopenicillanoyloxymethylpenicillanate 1,1-dioxide in 25 ml. of chloroform is added 1.50 ml. oftriethylamine. The mixture is cooled to 0° C., and a solution of 1.55 g.of 2-phenylacetyl chloride in 10 ml. of chloroform is added dropwise at0° C. The resulting mixture is stirred for 5 minutes at 0° C. and thenfor 30 minutes at 25° C. The solvent is removed by evaporation in vacuoand the residue is partitioned between ethyl acetate and water at pH 8.The ethyl acetate layer is removed, washed with water, dried (Na₂ SO₄)and evaporated in vacuo, to give the title compound.

EXAMPLE 16 6'-(2-Phenoxyacetamido)penicillanoyloxymethyl Penicillanate1,1-Dioxide

The title compound is prepared by acylation of6'-aminopenicillanoyloxymethyl penicillanate 1,1-dioxide with2-phenoxyacetyl chloride, according to the procedure of Example 15.

EXAMPLE 17 6'-(2-Amino-2-phenylacetamido)penicillanoyloxymethylPenicillanate 1,1-Dioxide

To a stirred solution of 155.2 g. of potassiumN-(1-methyl-2-ethoxycarbonylvinyl)-D-2-amino-2-phenylacetate hemihydrate(Chem. Ber., 98, 789 [1965]) in 2,000 ml. of ethyl acetate is added 2.5ml. of N-methylmorpholine and 70 ml. of isobutyl chloroformate, at -15°C. Stirring is continued at -15° C. for 15 minutes, an then a solutionof 231 g. of 6'-aminopenicillanoyloxymethyl penicillanate 1,1-dioxide in1,000 ml. of ethyl acetate is added, dropwise, at -15° C., over a periodof 15 minutes. Stirring is continued at 15° C. for 1 hour and then thereaction mixture is allowed to warm to room temperature. At this pointthe reaction mixture is washed with water, aqueous sodium bicarbonate(0.5 M) and again with water. The ethyl acetate solution is then driedand evaporated in vacuo. The residue is dissolved in 2,000 ml. of 1:1tetrahydrofuran-water and the pH is adjusted to 2.5. The solution isstirred at a pH of 2.5 for 1 hour, and then the bulk of thetetrahydrofuran is removed by evaporation in vacuo. The pH of theaqueous phase is adjusted to 8.5, and then the aqueous phase isextracted with ethyl acetate. The extracts are washed with water, dried(Na₂ SO₄) and evaporated in vacuo to give the title compound.

EXAMPLE 186'-(2-Amino-2-[4-hydroxyphenyl]acetamido)penicillanoyloxymethylPenicillanate 1,1-Dioxide

The title compound is prepared from 6'-aminopenicillanoyloxymethylpenicillanate 1,1-dioxide and sodiumN-(1-methyl-2-methoxycarbonylvinyl)-D-2-amino-2-(4-hydroxyphenyl)acetate(Journal of the Chemical Society [London] Part C, 1920 [1971]), usingthe procedure of Example 17.

EXAMPLE 19 6'-(2-Carboxy-2-phenylacetamido)penicillanoyloxymethylPenicillanate 1,1-Dioxide

To a stirred solution of 2.31 g. of 6'-aminopenicillanoyloxymethylpenicillanate 1,1-dioxide in 15 ml. of ethyl acetate is added 0.605 g.of N,N-dimethylaniline at 0° C. The temperature is maintained at 0° C.,and 30 ml. of a 0.2 molar solution of phenylmalonyl chloridetrimethylsilyl ester is added dropwise during 5 minutes. The reactionmixture is washed with water, and then an equal volume of fresh water isadded. The pH of the aqueous phase is adjusted to 7.0 with saturatedsodium bicarbonate and the layers are separated. The organic layer isdiscarded, and fresh ethyl acetate is added to the aqueous layer. The pHof the aqueous layer is lowered to 3.5, and again the layers areseparated. The ethyl acetate layer is dried (Na₂ SO₄) and evaporated invacuo to give the title compound.

The 0.2 molar solution of phenylmalonyl chloride trimethylsilyl ester isprepared according to Preparation A of U.S. Pat. No. 3,862,933.

EXAMPLE 20 6'-(2-Carboxy-2-[3-thienyl]acetamido)penicillanoyloxymethylPenicillanate 1,1-Dioxide

The title compound is prepared by acylation of6'-aminopenicillanoyloxymethyl penicillanate 1,1-dioxide with[3-thienyl]malonyl chloride trimethylsilyl ester, following theprocedure of Example 19. [3-Thienyl]malonyl chloride trimethylsilylester is prepared according to the method of U.S. Pat. No. 3,862,933.

EXAMPLE 21 6'-(2-Carboxy-2-[2-thienyl)acetamido)penicillanoyloxymethylPenicillanate 1,1-Dioxide

The pH of a stirred suspension of 372 mg. of 2-[2-thienyl]malonic acidin 10 ml. of water and 5 ml. of tetrahydrofuran is adjusted to 6.0 bythe addition of saturated sodium bicarbonate solution. To the resultingsolution is added 923 mg. of 6'-aminopenicillanoyloxymethylpenicillanate 1,1-dioxide. The mixture is cooled to ca. 0° C., and 402mg. of N-ethyl-N'-3-(dimethylamino)propylcarbodiimide hydrochloride isadded, with stirring. Stirring is continued at ca 0° C. for 5 minutesand at 25° C. for 2 hours, the pH continuously being maintained between5.8 and 6.0. At this point, the bulk of the tetrahydrofuran is removedby evaporation in vacuo, ethyl acetate and additional water are addedand the pH is raised to 8.0. The layers are separated and the organiclayer is discarded. Fresh ethyl acetate is added, and the pH is loweredto 3.0. Again the layers are separated, and the ethyl acetate layer isdried (Na₂ SO₄) and evaporated in vacuo. This affords the titlecompound.

EXAMPLE 226'-(2-[4-Ethyl-2,3-dioxopiperazinocarbonylamino]-2-phenylacetamido)penicillanoyloxymethylPenicillanate 1,1-Dioxide

To a stirred mixture of 3.19 g. of2-(4-ethyl-2,3-dioxopiperazinocarbonylamino)-2-phenylacetic acid in 50ml. of acetone is added 1.2 ml. of N-methylmorpholine. The resultingmixture is cooled to -20° C., and a solution of 1.09 g. of ethylchloroformate in 20 ml. of acetone is added dropwise during 10 minutes.Stirring is continued at -20° C. for 60 minutes, and then a solution of4.61 g. of 6'-aminopenicillanoyloxymethyl penicillanate 1,1-dioxide in50 ml. of acetone is added dropwise at -20° C. Stirring is continued at-20° C. for 60 minutes, at 0° C. for 30 minutes and at 25° C. for 30minutes. At this point the solvent is removed by evaporation in vacuo,and the residue is partitioned between ethyl acetate and water at pH2.5. The layers are separated and the aqueous layer is discarded. Freshwater is added and the pH is raised to 8.5. The layers are shaken andseparated, and then the organic layer is discarded. Fresh ethyl acetateis added and the pH is again adjusted to 2.5. The layers are shaken andseparated. The ethyl acetate layer is washed with water, and then it isdried. Evaporation of the ethyl acetate layer is vacuo affords the titlecompound.

EXAMPLE 23

The procedure of Example 22 is repeated, except that the2-(4-ethyl-2,3-dioxopiperazinocarbonylamino)-2-phenylacetic acid isreplaced by:

2-(2-oxoimidazolidinocarbonylamino)-2-phenylacetic acid,

2-(3-acetyl-2-oxoimidazolidinocarbonylamino)-2-phenylacetic acid,

2-(3-butyryl-2-oxoimidazolidinocarbonylamino)-2-phenylacetic acid,

2-(3-methylsulfonyl-2-oxoimidazolidinocarbonylamino)-2-phenylacetic acidand

2-(3-isopropylsulfonyl-2-oxoimidazolidinocarbonylamino)-2-phenylaceticacid, respectively. This affords:

6'-(2-[2-oxoimidazolidinocarbonylamino]-2-phenylacetamido)penicillanoyloxymethylpenicillanate 1,1-dioxide,

6'-(2-[3-acetyl-2-oxoimidazolidinocarbonylamino]-2-phenylacetamido)penicillanoyloxymethylpenicillanate 1,1-dioxide,

6'-(2-[3-butyryl-2-oxoimidazolidinocarbonylamino]-2-phenylacetamido)penicillanoyloxymethylpenicillanate 1,1-dioxide,

6'-(2-[3-methylsulfonyl-2-oxoimidazolidinocarbonylamino]-2-phenylacetamido)penicillanoyloxymethylpenicillanate 1,1-dioxide and

6'-(2-[3-isopropylsulfonyl-2-oxoimidazolidinocarbonylamino]-2-phenylacetamido)penicillanoyloxymethylpenicillanate 1,1-dioxide, respectively.

EXAMPLE 24 6'-Aminopenicillanoyloxymethyl Penicillanate 1,1-Dioxide

To a solution of 1.2 g. of6'-(4-nitrobenzyloxycarbonylamino)penicillanoyloxymethyl penicillanate1,1-dioxide in a mixture of 30 ml. of water and 50 ml. oftetrahydrofuran was added 1 drop of acetic acid (pH dropped to 4.5),followed by 1.2 g. of 10% palladium-on-carbon. The mixture was shakenunder an atmosphere of hydrogen, at ca. 50 psig pressure, for 1.5 hours.The mixture was then filtered and the residue was washed with water andwith tetrahydrofuran. The tetrahydrofuran-water, water andtetrahydrofuran solutions were combined and the pH was adjusted to 8.5.The resulting solution was extracted with ethyl acetate, and the ethylacetate extract was dried (Na₂ SO₄). The dried solution was evaporatedin vacuo giving 600 mg. of crude material.

The crude material was chromatographed on silica gel, eluting with 3:1ethyl acetate-hexane, which afforded 200 mg. of the title compound (23%yield). The IR spectrum (KBr disc) showed an absorption at 1783 cm⁻¹.The NMR spectrum (CDCl₃) showed absorptions at 5.9 (s), 5.5 (m), 4.63(m,), 4.5 (s), 3.5 (d), 1.7 (s), 1.6 (s), 1.5 (s) and 1.45 (s) ppm.

6'-Aminopenicillanoyloxymethyl penicillanate 1,1-dioxide will formacid-addition salts. The salts are prepared in conventional fashion,i.e. using the methods described earlier for the formation ofacid-addition salts of those compounds of formula I which have an aminogroup as part of the group R¹.

EXAMPLE 25 Chloromethyl Penicillanate 1,1-Dioxide

To a stirred solution of 24 g. of penicillanic acid 1,1-dioxide in 125ml. of N,N-dimethylformamide was added 9.5 ml. of diisopropylethylamine,followed by 45 ml. of chloroiodomethane. Stirring was continuedovernight and then the reaction mixture was added to 300 ml. of water.The pH was adjusted to 8.5, and then the mixture was extracted withethyl acetate. The extract was washed with water, followed by saturatedsodium chloride solution, and then it was dried over sodium sulfate. Thedried extract was concentrated to dryness in vacuo to give the crudeproduct as a gum (8.9 g.).

The crude product was combined with some additional material ofcomparable quality, and it was chromatographed on silica gel elutingwith 1:1 ethyl acetate-hexane. This afforded the title compound whichshowed only a single spot when assayed by thin-layer chromatography. TheIR spectrum (KBr disc) showed an absorption at 1801 cm⁻¹. The NMRspectrum (CDCl₃) showed absorptions at 6.0 (d, 1H, J=6 Hz), 5.7 (d, 1H,J=6 Hz), 4.7 (t, 1H, J=3.5 Hz), 4.5 (s, 1H), 3.55 (d, 2H, J=3.5 Hz), 1.7(s, 3H) and 1.5 (s, 3H) ppm.

EXAMPLE 26

The procedure of Example 25 is repeated, except that thechloroiodomethane used therein is replaced by an equimolar amount ofbromoiodomethane, diiodomethane, di(methylsulfonyloxy)methane,di(isobutylsulfonyloxy)methane, di(benzenesulfonyloxy)methane anddi(4-toluenesulfonyloxy)methane. This affords:

bromomethyl penicillanate 1,1-dioxide,

iodomethyl penicillanate 1,1-dioxide,

methylsulfonyloxymethyl penicillanate 1,1-dioxide,

isobutylsulfonyloxymethyl penicillanate 1,1-dioxide,

benzenesulfonyloxymethyl penicillanate 1,1-dioxide and

4-toluenesulfonyloxymethyl pencillanate 1,1-dioxide, respectively.

EXAMPLE 27 Chloromethyl6-(2-Benzyloxycarbonylamino-2-phenylacetamido)penicillanate

To a 1 liter 3-neck round bottom flask equipped with a magnetic stirrerand containing6-(2-benzyloxycarbonylamino-2-phenylacetamido)penicillanic acid (99.30g.) in dimethylsulfoxide (500 ml.) cooled to 15° C. was added dropwiseover a 15 minute period triethylamine (28.5 ml.). To this solution wasadded potassium iodide (2.0 g.) followed by the dropwise addition ofiodochloromethane (143 g.) over a 15 minute period. The reaction wasstirred at room temperature overnight. To this solution was added ethylacetate (1 liter). The resultant organic layer was washed with brine(3×300 ml.) and water (1×300 ml.). The combined aqueous wash wasreextracted with ethyl acetate (300 ml.). The ethyl acetate extractswere dried over magnesium sulfate, filtered and concentrated to afford116 g. of crude product. Silica gel (1 kg.) chromatography usingchloroform afforded 24.6 g. (23%) of the title compound as a lightyellow foam, m.p. 75°-77° C.

EXAMPLE 286'-(2-Benzyloxycarbonylamino-2-phenylacetamido)penicillanoyloxymethylPenicillanate 1,1-Dioxide

To a 500 ml. round bottom flask equipped with a paddle stirrer andcontaining chloromethyl6-(2-benzyloxycarbonylamino-2-phenylacetamido)penicillanate (20 g.) indimethylsulfoxide (120 ml.) at room temperature was added sodiumpenicillanate 1,1-dioxide (9.6 g.) followed by potassium iodide (600mg.). The reaction was allowed to stir overnight. An additional charge(2.4 g.) of sodium penicillanate 1,1-dioxide was added and the reactionmixture was stirred for an additional 6 hours. The crude reactionmixture was then poured into ice water (600 ml.) and extracted withethyl acetate (1×500 ml., 3×200 ml.). The organic extracts werebackwashed with water (2×500 ml.) and brine (1×500 ml.) and dried overmagnesium sulfate in the presence of activated carbon. The solution wasfiltered and concentrated in vacuo to afford 23.9 g. of crude product.Silica gel (250 g.) chromatography using chloroform afforded 14.5 g.(53%) of the title product, m.p. 80°-112° C.

EXAMPLE 29 6'-(2-Amino-2-phenylacetamido)penicillanoyloxymethylPenicillanate 1,1-Dioxide Hydrochloride

To a 500 ml. hydrogenation flask, containing6'-(2-benzyloxycarbonylamino-2-phenylacetamido)penicillanoyloxymethylpenicillanate 1,1-dioxide (5.50 g.) in tetrahydrofuran (75 ml.) wereadded water (75 ml.) acetic acid (1 drop) and 10% palladium on carbon(13.75 g.). The mixture was purged with nitrogen and then it was shakenunder an atmosphere of hydrogen at 47 psig pressure for 30 minutes. Anadditional catalyst charge (3.00 g.) was added and the mixture washydrogenated for an additional 15 minutes. The mixture was purged withnitrogen and filtered through a celite pad. The catalyst was washed withtetrahydrofuran (50 ml.) and water (30 ml.). The black solution wasrefiltered. 1.0 N Hydrochloric acid (7.54 ml.) was then added to theaqueous solution which was cooled to 0° C. The pH of this yellowsolution was 1.7. Tetrahydrofuran was then removed in vacuo and theresultant aqueous solution was saturated with sodium chloride andextracted with ether (2×100 ml.). The aqueous solution was thenreextracted with methylene chloride (5×50 ml.). The organic extractswere backwashed with saturated brine (2×50 ml.), dried over magnesiumsulfate and concentrated to ca. 100 ml. The crude product wasprecipitated with hexane (100 ml.) and filtered to afford 3.2 g. of acream colored solid. The crude product was redissolved in methylenechloride (50 ml.) and precipitated slowly with hexane (40 ml.) to affordafter drying (23°/1.6 mm.) 2.78 g. (58%) of the title product, m.p. 190°C.

PREPARATION 1 6-(2-Benzyloxycarbonylamino-2-phenylacetamido)penicillanicAcid

To a mixture of 100 ml. of water and 50 ml. of tetrahydrofuran was added10.1 g. of 6-(2-amino-2-phenylacetamido)penicillanic acid trihydrate andthen the pH was adjusted to 8.0. To the solution so obtained was addedbenzyl chloroformate (3.6 ml.), dropwise, with stirring, at a pH of8.0-8.5. Stirring was continued until the pH became stable, and then thesolution was extracted with ethyl acetate. The ethyl acetate extract wasdiscarded, and the pH of the aqueous phase was lowered to 2.0. Theacidified aqueous phase was extracted with ethyl acetate, and the latterorganic phase was dried and evaporated in vacuo. This afforded 11.4 g.of the title compound (94% yield). The NMR spectrum (CDCl₃ /DMSO-d₆)showed absorptions at 8.2 (d, 1H), 7.6-7.2 (m, 10H), 7.0-6.6 (m, 1H),5.6-5.3 (m, 3H), 5.1 (s, 2H), 4.3 (s, 1H) and 1.5 (2 s's, 6H) ppm.

PREPARATION 26-(2-Benzyloxycarbonylamino-2-[4-hydroxyphenyl]acetamido)penicillanicAcid

The title compound was prepared from6-(2-amino-2-[4-hydroxyphenyl]acetamido)penicillanic acid and benzylchloroformate, using the procedure of Preparation 1. Yield 97%. The NMRspectrum of the product (CDCl₃ /DMSO-d₆) showed absorptions at 7.6-7.0(m, 8H), 7.0-6.6 (d, 2H, J=8 Hz), 5.6-5.2 (m, 3H), 5.2-5.0 (s, 2H) and4.5 (broad s, 6H) ppm.

PREPARATION 36-(2-[4-Nitrobenzyloxycarbonylamino]-2-phenylacetamido)penicillanic Acid

The title compound was prepared from6-(2-amino-2-phenylacetamido)penicillanic acid and 4-nitrobenzylchloroformate, using the procedure of Preparation 1.

The product thus obtained was partitioned between ethyl acetate andwater and the pH was adjusted to 8.5 using potassium hydroxide. Theethyl acetate layer was removed and discarded, and the aqueous phase waslyophilized. This afforded the potassium salt of the title compound.Yield 82%. The NMR spectrum (CDCl₃ /DMSO-d₆) showed absorptions at 8.2(d, 2H, J=8 Hz), 7.8-7.2 (m, 7H), 5.8-5.4 (m, 3H), 5.2 (s, 2H), 4.2 (s,1H), 4.0-3.6 (broad s, 2H) and 1.8-1.2 (m, 6H) ppm.

PREPARATION 46-(2-[4-Nitrobenzyloxycarbonylamino]-2-[4-hydroxyphenyl]acetamido)penicillanicAcid

The title compound was prepared from6-(2-amino-2-[4-hydroxyphenyl]acetamido)penicillanic acid and4-nitrobenzyl chloroformate, using the procedure of Preparation 1. Theproduct was converted into its potassium salt using the method describedin Preparation 3.

PREPARATION 5 Chloromethyl6-(2-Benzyloxycarbonylamino-2-phenylacetamido)penicillanate

A mixture of 1.04 g. of potassium6-(2-benzyloxycarbonylamino-2-phenylacetamido)penicillanate, 0.87 ml. ofchloroiodomethane and 10 ml. of N,N-dimethylformamide was stirred atambient temperature overnight. The reaction mixture was poured into 50ml. of water, and the pH was raised to 8.5. The acidified mixture wasextracted with ethyl acetate. The extracts were combined, washed withwater and then with saturated sodium chloride solution, and then theywere dried (Na₂ SO₄). Evaporation in vacuo gave 650 mg. (61% yield) ofthe title compound. The IR spectrum (KBr disc) showed an absorption at1802 cm⁻¹. The NMR spectrum (CDCl₃) showed absorptions at 7.4 (s, 10H),7.3-7.0 (m, 2H), 6.3 (d, 1H, J=7 Hz), 6.0-5.2 (m, 5H), 5.1 (s, 1H), 4.4(s, 1H) and 1.5 (m, 6) ppm.

PREPARATION 6 Chloromethyl6-(2-[4-Nitrobenzyloxycarbonylamino]-2-phenylacetamido)penicillanate

The title compound was prepared from potassium6-(2-[4-nitrobenzyloxycarbonylamino]-2-phenylacetamido)penicillanate andchloroiodomethane according to the procedure of Preparation 5. The yieldof crude product was 68%.

A quantity (2.1 g.) of the above crude product was chromatographed onsilica gel using 1:1 ethyl acetate-hexane as eluant, to give materialshowing only one spot when assayed by thin-layer chromatography.

PREPARATION 7 Chloromethyl6-(2-[4-Nitrobenzyloxycarbonylamino]2-[4-hydroxyphenyl]acetamido)penicillanate

The title compound was prepared from potassium6-(2-[4-nitrobenzyloxycarbonylamino]-2-[4-hydroxyphenyl]acetamido)penicillanateand chloroiodomethane according to the procedure of Preparation 5. Theyield of crude product was 68%.

The crude product was chromatographed on silica gel using 2:1 ethylacetate-hexane as eluant, to give a 29% yield of material showing onlyone spot when assayed by thin-layer chromatography. The NMR spectrum(CDCl₃) showed absorptions at 8.2 (d, 2H, J=8 Hz), 7.7-7.0 (m, 6H),6.9-6.3 (m, 3H), 6.0-5.3 (m, 5H), 5.2 (s, 2H), 4.4 (s, 1H) and 1.5 (d,6H) ppm.

PREPARATION 8 6'-(4-Nitrobenzyloxycarbonylamino)penicillanoyloxymethylPenicillanate 1,1-Dioxide

To a stirred solution of 4.32 g. of potassium6-(4-nitrobenzyloxycarbonylamino)penicillanate in 60 ml. of dimethylsulfoxide was added 2.53 g. of chloromethyl penicillanate 1,1-dioxide,followed by a few milligrams of sodium iodide. Stirring was continuedfor 16 hours, and then the mixture was poured in 200 ml. of water. ThepH was adjusted to 8.5, and the resulting mixture was extracted withethyl acetate. The ethyl acetate extracts were washed with waterfollowed by saturated sodium chloride solution. The resulting solutionwas evaporated in vacuo to give 1.57 g. of crude material.

The crude material was chromatographed on silica gel, eluting with ethylacetate, to give 1.2 g. of the title compound. The NMR spectrum showedabsorptions at 8.25 (d), 7.50 (d), 5.95 (s), 5.73 (m), 5.55 (broad s),5.23 (s), 4.75 (t), 4.46 (s), 4.44 (s), 3.46 (s), 3.44 (s), 1.72 (s),1.65 (s), 1.52 (s) and 1.40 (s) ppm.

PREPARATION 9 6-(2-Benzyloxycarbonylamino-2-phenylacetamido)penicillanicAcid

To a 3 liter 3-neck round bottom flask equipped with a paddle stirrerand containing 6-(2-amino-2-phenylacetamido)penicillanic acid trihydrate(121.04 g.), tetrahydrofuran (550 ml.), and water (1000 ml.) cooled to5° C. was added 10% sodium hydroxide (˜108 ml.) until the pH was ˜7.7.Over a 45 minute period with cooling, benzylchloroformate (53.87 g.) and10% sodium hydroxide (˜108 ml.) were simultaneously added while the pHwas maintained between 8.0-8.5. The reaction mixture was stirred withcooling for an additional hour after completion of the addition. Thecrude reaction mixture was concentrated in vacuo to remove thetetrahydrofuran. The aqueous solution was extracted with ethyl acetate(2×250 ml.). This organic extract was discarded. The aqueous solutionwas cooled to 5° C., ethyl acetate (500 ml.) was added, and the pH wasadjusted to 2.0 using 6 N hydrochloric acid (50 ml.). The organic layerwas separated and the aqueous was reextracted with ethyl acetate (3×250ml.). The combined organic extracts were washed with brine (100 ml.),dried over magnesium sulfate, filtered and concentrated to afford crudeproduct which was slurried with ether and filtered. The ether filtratewas concentrated to afford a white foam which was slurried with hexaneand also filtered. The combined crude products were dried in vacuoovernight to yield 137.8 g. (95%) of the title compound, m.p. 144°-145°C.

I claim:
 1. The compound of the formula ##STR11## and the acid-additionsalts thereof.
 2. A compound of the formula ##STR12## wherein X isselected from the group consisting of chloro, bromo, iodo,alkylsulfonyloxy having from one to four carbons, benzenesulfonyloxy andtoluenesulfonyloxy.
 3. The compound according to claim 2, wherein X ischloro.